The Recall Desk

State

Utah product recalls

73,738 recalls have nationwide distribution and so reach Utah. 4,914 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total
4,914
Critical
524
Severe
1,350
Most recent
2026-10-28

Of the 4,914 recalls naming Utah we have scored against our rubric, 524 (11%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,350 (27%) are Severe.

These figures cover only the 4,914 recalls whose distribution notice names Utah specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30551–30575 of 78652

  • SevereNHTSA·20V344000·2020-06-11

    Vermeer Recalls 2020 Wood Chippers Due to Wheel Lug Nut Loosening

    Vermeer is recalling 2020 BC1200XL and BC1500 wood chippers because wheel lug nuts may loosen, allowing the wheel to detach and increasing crash risk.

    Product
    VERMEER — VERMEER BC1200XL, BC1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E038000·2020-06-11

    Dana Heavy Vehicle Output Shafts Recalled for Fracture Risk

    Dana Incorporated is recalling certain heavy vehicle output shafts that may not have been properly heat treated, posing a risk of shaft fracture and detachment.

    Product
    POWER TRAIN:DRIVELINE:DRIVESHAFT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V343000·2020-06-11

    Jeep Cherokee Recall for Power Transfer Unit Spline Wear

    FCA US LLC is recalling 2014-2017 Jeep Cherokee vehicles due to a defect in the Power Transfer Unit that may cause loss of drive or Park function.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E037000·2020-06-11

    Chrysler Recalls Jeep Cherokee Power Transfer Units for Drive Loss Risk

    Chrysler is recalling specific Two-Speed Power Transfer Units for Jeep Cherokee vehicles because worn splines can cause a loss of drive or Park function, increasing crash risk.

    Product
    POWER TRAIN:DRIVELINE:DIFFERENTIAL UNIT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20135·2020-06-11

    Bonnsu Recalls Miniware Teething Spoons Due to Choking Hazard

    Bonnsu is recalling Miniware teething spoons because they can break in an infant's mouth, posing a choking hazard. One injury report has been received.

    Product
    Miniware Teething Spoons
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V345000·2020-06-11

    Lode King Prestige Semi-Trailer Recalled for Incorrect Load Rating Decal

    Lode-King is recalling one 2021 Prestige SDG semi-trailer because the load rating decal exceeds the frame's strength capability, increasing crash risk if overloaded.

    Product
    LODE KING — LODE KING PRESTIGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20750·2020-06-11

    Davina Wellness Recalls Wintergreen Essential Oils Due to Packaging Defect

    Davina Wellness is recalling wintergreen essential oils because the packaging is not child-resistant, posing a risk of poisoning to young children.

    Product
    Davina Wintergreen Essential Oil and Davina Kneads Relief Sore Muscle Blend
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1299-2020·2020-06-10

    Acella Recalls NP Thyroid 15 Tablets Due to Superpotent Drug Risk

    Acella Pharmaceuticals is voluntarily recalling 29,304 bottles of NP Thyroid 15 tablets because the drug is superpotent. The recall covers products distributed nationwide in the US and Puerto Rico.

    Product
    NP THYROID 15 — NP THYROID 15 (LEVOTHYROXINE, LIOTHYRONINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1298-2020·2020-06-10

    Acella Recalls Superpotent NP Thyroid 15 Tablets Nationwide

    Acella Pharmaceuticals is voluntarily recalling 112,140 bottles of NP Thyroid 15 tablets because the drug is superpotent. The recall covers distribution across the US and Puerto Rico.

    Product
    NP THYROID 15 — NP THYROID 15 (LEVOTHYROXINE, LIOTHYRONINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0974-2020·2020-06-10

    KFK Organic Ground Oregano Recalled for Undeclared Tree Nuts and Crustacea

    K F K Seasonings Llc is recalling Organic Ground Oregano due to undeclared tree nuts and Crustacea. The product was distributed in Oregon and Utah.

    Product
    Organic Ground Oregano, Item # 90206. Packaged in 40 lbs. or 50 lbs. cases and sold under brand KFK Seasoning. This product contains Organic Oregano.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-1300-2020·2020-06-10

    Acella Recalls Superpotent NP Thyroid 15 Thyroid Tablets Nationwide

    Acella Pharmaceuticals is voluntarily recalling 49,128 bottles of NP Thyroid 15 tablets because they are superpotent. The FDA classified this as a Class I recall.

    Product
    NP THYROID 15 — NP THYROID 15 (LEVOTHYROXINE, LIOTHYRONINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2219-2020·2020-06-10

    Zimmer Biomet Recalls Vital MIS Spinal Fixation Implants Due to Locking Issues

    Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because the extended tab screws may not lock properly, causing the closure top to back out after surgery.

    Product
    Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 6.5X35MM, Item Number 810M6535 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2210-2020·2020-06-10

    Zimmer Biomet Recalls Vital MIS Spinal Fixation Implants Due to Locking Issues

    Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because the extended tab screws may not lock properly, causing the closure top to back out after surgery.

    Product
    Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 4.5X30MM, Item Number 810M4530 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2205-2020·2020-06-10

    Umano Medical Recalls AC Powered Hospital Adjustable Beds

    Umano Medical is recalling 3,259 AC powered hospital adjustable beds due to a potential hazard of unsupervised patients falling out of bed.

    Product
    AC Powered hospital adjustable bed.
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2261-2020·2020-06-10

    Spacelabs Xhibit Central Recall for Audio Alarm Loss After Power Failure

    Spacelabs Healthcare is recalling Xhibit Central software due to reports of audio alarm loss after power failures or cable disconnections, which could delay alarm recognition.

    Product
    Xhibit Central, Model No. 96102 - Product Usage: intended use is to provide clinicians with central monitoring of adult, pediatric and neonatal patient data of patients connected to networked Spacelabs Healthcare patient monitors and telemetry transmitters.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2258-2020·2020-06-10

    GE Healthcare Recalls Nuclear Medicine Systems Due to Software Defect

    GE Healthcare is recalling 526 Nuclear Medicine systems because outdated software caused a patient's finger to be injured during an automatic unload process.

    Product
    System, Tomography Computed Emmission
    Category
    Medical Device
    Distribution
    40 states
  • SevereFDA (Food)·F-0972-2020·2020-06-10

    K F K Seasonings Recalls Azure Market Chili Powder for Undeclared Allergens

    K F K Seasonings LLC is recalling 96 lbs of Azure Market Chili Powder, Mild, Organic due to undeclared tree nuts and Crustacea.

    Product
    Chili Powder, Mild, Organic is a blend, Item # 90030. Packaged in 1 lb. bags and sold under brand Azure Market. This product contains "Organic Chili Peppers, Salt, Organic Spices, Organic Garlic, Organic Sunflower Oil". The Azure Market label listed the lot # 90030041520 and…
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2257-2020·2020-06-10

    Siemens ARTIS icono X-Ray Systems Recalled for Incorrect Vessel Quantification

    Siemens is recalling five ARTIS icono X-ray systems because software may fail to detect vessels or provide incorrect measurements, potentially leading to wrong diagnoses.

    Product
    ARTIS icono systems with Quantification Application SW (QVA/QCA) on a standalone XWP computer, an interventional Fluoroscopic X-Ray System Model Number: 11327600
    Category
    Medical Device
    Distribution
    4 states
  • SevereFDA (Devices)·Z-2174-2020·2020-06-10

    FDA Recalls Sterile Surgical Packs Due to Unregistered Facility

    American Contract Systems is recalling 2,868 sterile surgical packs because they were manufactured in a facility not registered by the FDA.

    Product
    Sterile Custom Packs to be used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V341000·2020-06-10

    KME Fire Trucks Recalled for Potential Braking Mechanism Separation

    KME is recalling specific fire trucks because the optional Telma induction braking mechanism may separate from the vehicle while moving, increasing crash risk.

    Product
    KME — KME PREDATOR PANTHER, PREDATOR SS, PREDATOR, COMMERCIALCAB/ CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2231-2020·2020-06-10

    Zimmer Biomet Recalls Vital MIS Spinal Fixation Implants Due to Locking Issues

    Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because the extended tab screws may not lock adequately, causing the closure top to back out after surgery.

    Product
    Vital MIS Spinal Fixation system implants CANN BL POLY EXT 8.5X55MM, Item Number 811M8555 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0973-2020·2020-06-10

    K F K Seasonings Recalls Organic Chipotle Chile Ground for Undeclared Tree Nuts

    K F K Seasonings is recalling 230 lbs of Organic Chipotle Chile Ground sold as Blue Chip in Oregon and Utah due to undeclared tree nuts.

    Product
    Organic Chipotle Chile Ground, Item # 90033. Packaged in 40 lbs. box and sold under brand Blue Chip. This product contains Chipotle Chile pepper. The Blue Chip label listed the lot # 032918. No UPC. Product distributed by Blue Chip Corp. UT.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2228-2020·2020-06-10

    Zimmer Biomet Recalls Vital MIS Spinal Fixation Implants Due to Locking Issues

    Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because reports indicate the extended tab screws may not lock adequately, causing the closure top to back out after surgery.

    Product
    Vital MIS Spinal Fixation system implants CANN BL POLY EXT 8.5X40MM, Item Number 811M8540 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is…
    Category
    Medical Device
    Distribution
    Distributed nationwide